Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs440446
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs440446
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs440446
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2011 2011
dbSNP: rs440446
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 1.000 1 2019 2019
dbSNP: rs440446
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 1.000 1 2019 2019
dbSNP: rs440446
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60
CUI: C0497327
Disease: Dementia
Dementia 		0.010 < 0.001 1 2019 2019
dbSNP: rs440446
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		0.010 < 0.001 1 2019 2019
dbSNP: rs440446
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2019 2019